My name is Misha Panesar, and I founded this registered nonprofit in honor of a loved one who recently underwent heart surgery for a defect they had since birth. For years, doctors never looked closely enough, and by the time it was finally discovered, it had become critical.

That experience showed me how many families are overlooked when it comes to heart health. Too often, people are told they are fine when something serious is being missed. I started this foundation so that no one else has to go through the same pain, fear, and silence that my family faced.

As a registered nonprofit, our mission is to:

Raise awareness about congenital heart defects so families know the warning signs.

Provide resources and education that guide families through testing, diagnosis, and care.

Host community events and workshops that bring people together to learn, connect, and support each other.

Advocate for earlier detection and better medical attention for those at risk.

Support patients and families during surgery and recovery with compassion and practical help.

Every donation to this campaign directly supports our nonprofit programs, events, and outreach. Together, we can ensure that every heartbeat is valued, every family feels supported, and no one is left unheard.

Thank you for believing in this mission and helping us bring hope and change to the community. ❤️